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Quality Level
assay
98%
form
solid
bp
236 °C (lit.)
mp
28-32 °C (lit.)
functional group
bromo
SMILES string
Oc1cccc(Br)c1
InChI
1S/C6H5BrO/c7-5-2-1-3-6(8)4-5/h1-4,8H
InChI key
MNOJRWOWILAHAV-UHFFFAOYSA-N
Gene Information
human ... ALOX12(239) , ALOX15(246)
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General description
3-Bromophenol is used for suzuki-miyaura coupling reaction and in the synthesis of pentacyclic building block benzodibenzofuranquinone.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
No data available
flash_point_c
No data available
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Toxicology, 30(3), 259-272 (1984-04-02)
Bromobenzene, at doses greater than 5.7 mmol/kg, produced renal proximal tubular necrosis and renal functional changes in mice. p-Bromophenol and o-bromophenol were the major urinary phenolic bromobenzene metabolites although m-bromophenol and 4-bromocatechol were also excreted in detectable quantities. With the
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 78(2), 575-581 (2010-12-28)
The FT-IR and FT-Raman spectra of 3-Bromo phenol (3-BP) molecule have been recorded using Bruker IFS 66V spectrometer in the range of 4000-100 cm(-1). The molecular geometry and vibrational frequencies in the ground state are calculated by using the ab
Drug metabolism and disposition: the biological fate of chemicals, 15(6), 857-867 (1987-11-01)
Premercapturic acids derived from bromobenzene 3,4-oxide were found to act as precursors of 3- and 4-bromophenol in the rat and guinea pig. The 4-S- and 3-S- positional isomers used in this study were rat urinary metabolites and were prepared in
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